1. A complex double translocation involving four chromosomes and five breakpoints in a child with mild mental retardation. Issue 5 (October 1983) Authors: Couzin, D A; Watt, J L; Auchterlonie, I A Journal: Journal of medical genetics Issue: Volume 20:Issue 5(1983) Page Start: 389 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A familial insertion involving an active nucleolar organiser within chromosome 12. Issue 5 (October 1984) Authors: Watt, J L; Couzin, D A; Lloyd, D J; Stephen, G S; McKay, E Journal: Journal of medical genetics Issue: Volume 21:Issue 5(1984) Page Start: 379 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A familial pericentric inversion of chromosome 22 with a recombinant subject illustrating a 'pure' partial monosomy syndrome. Issue 4 (August 1985) Authors: Watt, J L; Olson, I A; Johnston, A W; Ross, H S; Couzin, D A; Stephen, G S Journal: Journal of medical genetics Issue: Volume 22:Issue 4(1985) Page Start: 283 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A paracentric inversion of 7q illustrating a possible interchromosomal effect. Issue 4 (August 1986) Authors: Watt, J L; Ward, K; Couzin, D A; Stephen, G S; Hill, A Journal: Journal of medical genetics Issue: Volume 23:Issue 4(1986) Page Start: 341 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. De novo translocation heterozygote with three reciprocal translocations. Issue 5 (October 1983) Authors: Watt, J L; Couzin, D A Journal: Journal of medical genetics Issue: Volume 20:Issue 5(1983) Page Start: 385 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Interstitial deletion of chromosome 13: prognosis and adult phenotype. Issue 8 (August 1991) Authors: Dean, J C; Simpson, S; Couzin, D A; Stephen, G S Journal: Journal of medical genetics Issue: Volume 28:Issue 8(1991) Page Start: 533 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Partial trisomy 7 (q32----qter) syndrome in two children. Issue 5 (October 1986) Authors: Couzin, D A; Haites, N; Watt, J L; Johnston, A W Journal: Journal of medical genetics Issue: Volume 23:Issue 5(1986) Page Start: 461 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Prenatal detection of Turner's syndrome in conjunction with trisomy 20 mosaicism (45, X/46, X, +0). Issue 3 (June 1981) Authors: Watt, J L; Couzin, D A; Johnston, A W; Jandial, V; Gray, E S Journal: Journal of medical genetics Issue: Volume 18:Issue 3(1981) Page Start: 225 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Structural rearrangements in the parents of children with primary trisomy 21. Issue 5 (May 1987) Authors: Couzin, D A; Watt, J L; Stephen, G S Journal: Journal of medical genetics Issue: Volume 24:Issue 5(1987) Page Start: 280 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗